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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/30780
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dc.contributor.authorV. Suvatteen_US
dc.contributor.authorC. Wasien_US
dc.contributor.authorU. Kositanonten_US
dc.contributor.authorS. Bukkavesaen_US
dc.contributor.authorV. S. Tanphaichitren_US
dc.contributor.authorK. Chatiyanondaen_US
dc.contributor.authorN. Sangkavibhaen_US
dc.contributor.authorP. Tongcharoenen_US
dc.contributor.authorM. Takahashien_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-12T07:48:41Z-
dc.date.available2018-10-12T07:48:41Z-
dc.date.issued1985-12-01en_US
dc.identifier.citationAsian Pacific Journal of Allergy and Immunology. Vol.3, No.1 (1985), 16-22en_US
dc.identifier.issn0125877Xen_US
dc.identifier.other2-s2.0-0022347153en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0022347153&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/30780-
dc.description.abstractLive attenuated varicella vaccine (OKA strain) was administered to 42 children ranging in age from three to 13 years, they consisted of nine controls, 21 children on chemotherapy for acute leukaemia and lymphoma, and 12 children receiving steroid treatment. The immunisation was performed without suspending the administration of immunosuppressive agents in an attempt to stop the spread of varicella infection that was occurring at the time in the pediatric ward. After vaccination, seven immunocompromised children developed clinical varicella within 16-41 days. The symptoms were mild to moderate in all except one who had severe disseminated clinical symptoms. The attempt to isolate and identify vaccine virus markers in these patients was not successful, but there was no further spread of varicella in the paediatric ward. The overall seroconversion rate as determined by immune adherence haemagglutination test was found in 85 per cent of the vaccinees at three months after vaccination and significant antibody level persisted for 15 months in 60 per cent of them. Children with acute leukaemia and lymphoma had a good antibody response (93.3%) which was similar to that of normal children (75%) even without suspending cytotoxic drugs at the time of vaccination. Poorer antibody response (50%) was found in children who received steroid treatment. Positive skin test to varicella antigen was found in 50 per cent of the vaccinees at one month after vaccination; it declined to 31.5 per cent at six months. Only 6.2 per cent of the vaccinees had a positive skin reaction at 9-12 months. It was concluded that live attenuated varicella vaccine (OKA strain) is sufficiently safe and immunogenic in immunocompromised children even without suspending immunosuppressive agents at the time of vaccination. In addition, this vaccine was found to be effective for preventing the spread of varicella in the paediatric ward.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0022347153&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleLive attenuated varicella vaccination in immunocompromised childrenen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 1969-1990

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